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FDA Inspection 1094836 — Sanofi-Aventis Deutschland GmbH

Sanofi-Aventis Deutschland GmbH — FEI 3003195501

The FDA completed an inspection of Sanofi-Aventis Deutschland GmbH on May 14, 2019 in Frankfurt Am Main. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
May 14, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Frankfurt Am Main (Germany)

Facility

Other inspections at this facility

  • 1215824 (VAI Fri Mar 25 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1006001 (VAI Fri Mar 03 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 952968 (NAI Thu Dec 10 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 933399 (VAI Fri Jun 26 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 859523 (NAI Thu Dec 05 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources